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2. Clinical features and classification of the muscular dystrophies. Gardner-Medwin D Br Med Bull; 1980 May; 36(2):109-15. PubMed ID: 7020835 [No Abstract] [Full Text] [Related]
4. Distal muscular dystrophy in an English family. Sumner D; Crawfurd MD; Harriman DG Brain; 1971; 94(1):51-60. PubMed ID: 5552164 [No Abstract] [Full Text] [Related]
5. [Myopathia distalis tarda hereditaria. Results of a genealogical, clinical, clinical-chemical and electromyographic family study]. Bachmann H; Wagner A Psychiatr Neurol Med Psychol (Leipz); 1980 Jan; 32(1):20-8. PubMed ID: 7384294 [TBL] [Abstract][Full Text] [Related]
6. Single fiber electromyography in the differential diagnosis of myopathic limb girdle syndromes and chronic spinal muscular atrophy. Shields RW Muscle Nerve; 1984 May; 7(4):265-72. PubMed ID: 6727909 [TBL] [Abstract][Full Text] [Related]
7. Quadriceps myopathy in two brothers: rare familial myopathy confirmed by muscle biopsy. Finelli PF R I Med J (1976); 1979 Apr; 62(4):125-9. PubMed ID: 286404 [No Abstract] [Full Text] [Related]
8. [Charcot-Marie neural amyotrophy (review)]. Savchenko IuN Zh Nevropatol Psikhiatr Im S S Korsakova; 1984; 84(11):1718-22. PubMed ID: 6098115 [No Abstract] [Full Text] [Related]
9. [Clinical electroneuromyographic study of secondary neuromuscular syndromes]. Badalian LO; Dunaevskaia GN; Skvortsov IA Klin Med (Mosk); 1981 Mar; 59(3):16-20. PubMed ID: 7022001 [No Abstract] [Full Text] [Related]
10. [Muscular disease of X-linked autosomal recessive transmission with early muscular retractions and cardiac conduction disorders]. Serratrice G; Pouget J; Pellissier JF; Gastaut JL; Cros D Rev Neurol (Paris); 1982; 138(10):713-24. PubMed ID: 6891495 [No Abstract] [Full Text] [Related]
11. Hypotonia in infancy. Dubowitz V Acta Univ Carol Med Monogr; 1976; (75):13-8. PubMed ID: 1077757 [No Abstract] [Full Text] [Related]
12. A late autosomal dominant form of limb-girdle muscular dystrophy. A clinical, genetic, and morphological study. De Coster W; De Reuck J; Thiery E Eur Neurol; 1974; 12(3):159-72. PubMed ID: 4426323 [No Abstract] [Full Text] [Related]
13. [Principles and significance of clinical electromyography]. Schmoigl S Wien Med Wochenschr; 1971 Mar; 121(13):250-5. PubMed ID: 5560230 [No Abstract] [Full Text] [Related]
14. [Value of myometric findings in the morphological differential diagnosis of neuromuscular disorders (author's transl)]. Pongratz D Microsc Acta Suppl; 1980; Suppl 4():38-43. PubMed ID: 6931279 [TBL] [Abstract][Full Text] [Related]
16. [Distal myopathies: critical study and report on one case (author's transl)]. Serratrice G; Pellissier JF; Pouget J Ann Med Interne (Paris); 1982; 133(3):192-9. PubMed ID: 7103305 [TBL] [Abstract][Full Text] [Related]
17. [Facioscapulohumeral neuromuscular syndromes--problems of differential and early diagnosis and genetic counseling]. Bachmann H; Ziegan J; Steinbicker V; von Rohden L; Wagner A Psychiatr Neurol Med Psychol (Leipz); 1989 Oct; 41(10):586-95. PubMed ID: 2608758 [TBL] [Abstract][Full Text] [Related]
18. Correlation between electromyographic findings and muscle biopsy in ccases of neuromuscular diseease. Hausmanowa-Petrusewicz I; Jedrzejowska H J Neurol Sci; 1971 May; 13(1):85-106. PubMed ID: 5566111 [No Abstract] [Full Text] [Related]
19. [On the clinical aspects of the distal late myopathy (myopathia distalis tarda hereditaria Welander)]. Kaeser HE; Wurmser P Schweiz Med Wochenschr; 1967 Sep; 97(37):1208-11. PubMed ID: 5593061 [No Abstract] [Full Text] [Related]
20. Type I muscle fibre atrophy and central nuclei. A rare familial neuromuscular disease. Karpati G; Carpenter S; Nelson RF J Neurol Sci; 1970 May; 10(5):489-500. PubMed ID: 4910660 [No Abstract] [Full Text] [Related] [Next] [New Search]